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768335-42-8

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768335-42-8 Usage

General Description

(2R,6R)-2,6-dimethyl-piperazine is an organic compound that belongs to the class of piperazines. It has a molecular formula C6H14N2 and a molecular weight of 114.19 g/mol. This chemical is a clear, colorless liquid at room temperature with a boiling point of 110-112 °C. (2R,6R)-2,6-dimethyl-piperazine is commonly used as a building block in organic synthesis and in the manufacture of pharmaceuticals, agrochemicals, and other specialty chemicals. It has also been studied for its potential antimicrobial, antiviral, and anticancer properties. Additionally, it has applications in the field of materials science and is used as a solvent and in chemical reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 768335-42-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,8,3,3 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 768335-42:
(8*7)+(7*6)+(6*8)+(5*3)+(4*3)+(3*5)+(2*4)+(1*2)=198
198 % 10 = 8
So 768335-42-8 is a valid CAS Registry Number.

768335-42-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,6R)-2,6-dimethylpiperazine

1.2 Other means of identification

Product number -
Other names (2R,6R)-2,6-dimethylpiperazine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:768335-42-8 SDS

768335-42-8Downstream Products

768335-42-8Relevant articles and documents

Asymmetric Synthesis of (2R,6R) and (2S,6S)-2,6-Dimethylpiperazine

Mickelson, John W.,Jacobsen, E. Jon

, p. 19 - 22 (1995)

The title compounds were prepared via two efficient routes.The first sequence utilized a diastereospecific triflate alkylation in the key bond forming step while the second method relied on a novel intramolecular Mitsunobu reaction to set the required stereochemistry.

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